Major Pharmaceuticals recalls 75 mcg levothyroxine tablets due to subpotent drug levels. This may not provide proper thyroid hormone treatment. Affected units have specific NDC and lot numbers.
Subpotent Drug
Major Pharmaceuticals is recalling levothyroxine sodium tablets that may not contain enough active ingredient. This could lead to inadequate thyroid hormone treatment if used without medical supervision.
The tablets contain less active thyroid hormone than intended. This means they might not work properly for treating thyroid hormone deficiency. The risk is not immediate harm but potential treatment failure.
People prescribed levothyroxine by a doctor who own these specific tablets. Those with thyroid conditions are most at risk of treatment failure.
Check for NDC code 0904-6951-61 with lot numbers N02172 (exp 07/2026) or N02296/N02288 (exp 12/2026). These tablets are only available by prescription.
Verify the NDC code and lot numbers on your prescription bottle to confirm if it's affected.
The recall states these tablets may have subpotent drug levels, meaning they might not provide proper thyroid hormone treatment. They are not safe for use without medical supervision.
Check for NDC code 0904-6951-61 with lot numbers N02172 (exp 07/2026) or N02296/N02288 (exp 12/2026). These tablets are only available by prescription.
The recall does not specify a remedy, so contact your doctor to discuss alternative treatment options.
We’ve drafted a message you can send Major Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0702-2026 — Major Pharmaceuticals Major Pharmaceuticals Hello, I own a Major Pharmaceuticals that is covered by recall D-0702-2026 from Major Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
